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<meta content="Sex allocation theory predicts that parents should bias their reproductive investments toward the offspring
sex generating the greatest fitness return. When females are the heterogametic sex (e.g., ZW in butterflies, some
lizards, and birds), production of daughters is associated with an increased risk of offspring inviability due to the
expression of paternal, detrimental recessives on the Z chromosome. Thus, daughters should primarily be produced
when mating with partners of high genetic quality. When female sand lizards (Lacerta agilis) mate with genetically
superior males, exhibiting high MHC Class I polymorphism, offspring sex ratios are biased towards daughters, possibly
due to recruitment of more Z-carrying oocytes when females have assessed the genetic quality of their partners. If
our study has general applicability across taxa, it predicts taxon-specific sex allocation effects depending on which
sex is the heterogametic one." name="eprints.abstract" />
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<meta content="Anderholm, S., M. Olsson, E. Wapstra, and K. Ryberg. 2004. Fit
and fat from enlarged badges: a field experiment on male sand
lizards. Proc. R. Soc. Lond. B (Suppl.) 271:S142–S144.
Boudejamadi, K., O. Martin, J.-C. Simon, and A. Estoup. 1999.
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animals. J. Genet. 12:101–109.
Hardy, I. C. W. 2002. Sex ratios: concepts and research methods.
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lizards. Herp. Rev. 27:71–72.
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S. Andersson, and H. Tegelstro¨m. 2000. Population size and
genetic diversity in sand lizard (Lacerta agilis) and adders (Vipera
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on their evolutionary trend. Amphibia-Reptilia 14:1–11.
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in reptiles. Pp. 503–564 in T. Birkhead and A. Møller,
eds. Sexual selection and sperm competition. Academic Press,
London.
———. 2001. Promiscuity in sand lizards (Lacerta agilis) and adder
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to females: a test of the infertility hypothesis using lizards. Evolution
51:1684–1688.
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offspring, sibling matings, and selection against inbreeding in
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1996b. Sperm selection by females. Nature 383:585.
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ticks, and travels: a test of the immunocompetencehandicap
hypothesis in free-ranging male sand lizards. Proc. R.
Soc. Lond. B 267:2339–2343.
Olsson, M., T. Madsen, J. Nordby, E. Wapstra, B. Ujvari, and H.
Wittsell. 2003. Major histocompatibility complex and mate
choice in sand lizards. Proc. R. Soc. Lond. B. (Suppl.) 270:
S254–S256.
Olsson, M., B. Ujvari, T. Madsen, T. Uller, and E. Wapstra. 2004a.
Haldane rules: costs of outbreeding at production of daughters
in sand lizards. Ecol. Lett. In press.
Olsson, M., T. Madsen, B. Ujvari, and E. Wapstra. 2004b. Fecundity
and MHC affects ejaculation tactics and paternity bias in sand
lizards. Evolution 58:906–909.
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lizards, and birds), production of daughters is associated with an increased risk of offspring inviability due to the
expression of paternal, detrimental recessives on the Z chromosome. Thus, daughters should primarily be produced
when mating with partners of high genetic quality. When female sand lizards (Lacerta agilis) mate with genetically
superior males, exhibiting high MHC Class I polymorphism, offspring sex ratios are biased towards daughters, possibly
due to recruitment of more Z-carrying oocytes when females have assessed the genetic quality of their partners. If
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    <h1 class="ep_tm_pagetitle">The role of Handane's rule in sex allocation</h1>
    <p style="margin-bottom: 1em" class="not_ep_block"><span class="person_name">Olsson, Mats</span> and <span class="person_name">Madsen, Thomas</span> and <span class="person_name">Uller, Tobias</span> and <span class="person_name">Wapstra, Erik</span> and <span class="person_name">Ujvari, Beata</span> (2005) <xhtml:em>The role of Handane's rule in sex allocation.</xhtml:em> Evolution, 59 (1). pp. 221-225. ISSN 0014-3820</p><p style="margin-bottom: 1em" class="not_ep_block"></p><table style="margin-bottom: 1em" class="not_ep_block"><tr><td valign="top" style="text-align:center"><a href="http://eprints.utas.edu.au/2099/1/2005_Olsson_et_al_Evolution_(Haldanes_rule).pdf"><img alt="[img]" src="http://eprints.utas.edu.au/style/images/fileicons/application_pdf.png" class="ep_doc_icon" border="0" /></a></td><td valign="top"><a href="http://eprints.utas.edu.au/2099/1/2005_Olsson_et_al_Evolution_(Haldanes_rule).pdf"><span class="ep_document_citation">PDF</span></a> - Full text restricted - Requires a PDF viewer<br />63Kb</td><td><form method="get" accept-charset="utf-8" action="http://eprints.utas.edu.au/cgi/request_doc"><input accept-charset="utf-8" value="2723" name="docid" type="hidden" /><div class=""><input value="Request a copy" name="_action_null" class="ep_form_action_button" onclick="return EPJS_button_pushed( '_action_null' )" type="submit" /> </div></form></td></tr></table><p style="margin-bottom: 1em" class="not_ep_block">Official URL: <a href="http://dx.doi.org/10.1111/j.0014-3820.2005.tb00908.x">http://dx.doi.org/10.1111/j.0014-3820.2005.tb00908.x</a></p><div class="not_ep_block"><h2>Abstract</h2><p style="padding-bottom: 16px; text-align: left; margin: 1em auto 0em auto">Sex allocation theory predicts that parents should bias their reproductive investments toward the offspring&#13;
sex generating the greatest fitness return. When females are the heterogametic sex (e.g., ZW in butterflies, some&#13;
lizards, and birds), production of daughters is associated with an increased risk of offspring inviability due to the&#13;
expression of paternal, detrimental recessives on the Z chromosome. Thus, daughters should primarily be produced&#13;
when mating with partners of high genetic quality. When female sand lizards (Lacerta agilis) mate with genetically&#13;
superior males, exhibiting high MHC Class I polymorphism, offspring sex ratios are biased towards daughters, possibly&#13;
due to recruitment of more Z-carrying oocytes when females have assessed the genetic quality of their partners. If&#13;
our study has general applicability across taxa, it predicts taxon-specific sex allocation effects depending on which&#13;
sex is the heterogametic one.</p></div><table style="margin-bottom: 1em" cellpadding="3" class="not_ep_block" border="0"><tr><th valign="top" class="ep_row">Item Type:</th><td valign="top" class="ep_row">Article</td></tr><tr><th valign="top" class="ep_row">Additional Information:</th><td valign="top" class="ep_row">The definitive version is available at www.blackwell-synergy.com&#13;
</td></tr><tr><th valign="top" class="ep_row">Keywords:</th><td valign="top" class="ep_row">Heterogamety, MHC polymorphism, sex ratio adjustment, sex-specific mortality (daughters)</td></tr><tr><th valign="top" class="ep_row">Subjects:</th><td valign="top" class="ep_row"><a href="http://eprints.utas.edu.au/view/subjects/270706.html">270000 Biological Sciences &gt; 270700 Ecology and Evolution &gt; 270706 Life Histories (incl. Population Ecology)</a></td></tr><tr><th valign="top" class="ep_row">ID Code:</th><td valign="top" class="ep_row">2099</td></tr><tr><th valign="top" class="ep_row">Deposited By:</th><td valign="top" class="ep_row"><span class="ep_name_citation"><span class="person_name">Dr Erik Wapstra</span></span></td></tr><tr><th valign="top" class="ep_row">Deposited On:</th><td valign="top" class="ep_row">15 Oct 2007 14:41</td></tr><tr><th valign="top" class="ep_row">Last Modified:</th><td valign="top" class="ep_row">09 Jan 2008 02:30</td></tr><tr><th valign="top" class="ep_row">ePrint Statistics:</th><td valign="top" class="ep_row"><a target="ePrintStats" href="/es/index.php?action=show_detail_eprint;id=2099;">View statistics for this ePrint</a></td></tr></table><p align="right">Repository Staff Only: <a href="http://eprints.utas.edu.au/cgi/users/home?screen=EPrint::View&amp;eprintid=2099">item control page</a></p>
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